Thermoplastic composition for use in high impact applications

ABSTRACT

A thermoplastic composition comprising from about 50 to about 99 by weight percent of a nylon 6,6 resin, from about 1 to about 50 by weight percent of a polymer performance modifier and about from 0.01 to about 25 by weight percent of a silicone based additive, wherein the silicone based additive comprises an ultrahigh molecular weight siloxane polymer that is unfunctionalized and non-reactive with the polyamide resin, wherein the thermoplastic composition has an impact strength value which is greater than the combination of the polyamide resin and the polymer performance modifier or the combination of the polyamide resin and the silicone based additive and wherein the thermoplastic composition has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and the polymer performance modifier.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 14/577,420, filed on Dec. 19, 2014, which is a Continuation-In-Part of U.S. application Ser. No. 13/950,722 filed on Jul. 25, 2013, which claims Priority to U.S. Provisional Application No. 61/675,990 filed on Jul. 26, 2012, and U.S. Provisional Application No. 61/737,481 filed on Dec. 14, 2012, all of which are incorporated herein by reference.

FIELD OF THE INVENTION

This disclosure relates to polyamide compositions with improved impact strength.

BACKGROUND OF THE INVENTION

Nylon polymers are desirable in many applications due to its outstanding elasticity, dye-fastness and high melting point. Nylon polymer commonly takes the form of pellets or flakes, which can be melted and shaped for use in plastic applications or extruded as fiber for use in yarn applications, such as apparel, carpet, airbags and outdoor gear.

In recent years Nylon resins have been utilized for automotive, electrical/electronics, industrial and consumer applications. In order to meet the performance standards for these applications, Nylon resins are commonly enhanced with additives such as impact modifiers or tougheners and mineral or synthetic reinforcements.

Impact modified Nylon compositions are useful for industrial applications because they generally possess good impact strength, stiffness, weld line strength. U.S. Pat. Nos. 4,346,194 and 6,579,581, herein incorporated by reference, teach nylon resins with impact modifying components. Common impact modifiers are elastomeric, olefinic copolymers grafted with carboxyl or carboxylate functional groups. It is desirable to have nylon compositions with a high impact strength and stiffness. However, it is well known and understood that improving the impact strength of a polymer composition with such known modifiers generally results in a proportional decrease in tensile strength. Due to this inverse relationship, to achieve a significant increase in impact strength for a composition, a corresponding decrease in tensile strength must also be expected. This can limit the use of impact modified nylon compositions when tensile strength requirements cannot be met.

Therefore, there is a need for thermoplastic molding compositions that possess increased impact strength and similar tensile strength to the base resin used in the composition.

SUMMARY OF THE INVENTION

The present invention relates to a thermoplastic composition that comprises a polyamide resin, a polymer performance modifier and a silicone based additive. The resulting thermoplastic composition has an impact strength that is greater than the combination of the polyamide resin and polymer performance modifier alone and a tensile strength that is comparable the polyamide resin.

In one embodiment of the present invention the thermoplastic composition comprises from about 25 to about 99 by weight percent of a polyamide resin; from about 1 to about 50 by weight percent of a polymer performance modifier; and about from 0.01 to about 25 by weight percent of a silicone based additive.

In another embodiment, the thermoplastic composition has an impact strength value which is greater than the combination of the polyamide resin and the polymer performance modifier or the combination of the polyamide resin and the silicone based additive.

In another embodiment, the thermoplastic composition has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and the polymer performance modifier.

In another embodiment, the silicone based additive comprises an ultrahigh molecular weight siloxane polymer.

In another embodiment, the ultrahigh molecular weight siloxane polymer is unfunctionalized and non-reactive with the polyamide resin.

In another embodiment, the polymer performance modifier comprises an elastomeric polyolefinic polymer functionalized with an unsaturated carboxylic anhydride.

In another embodiment, the polymer performance modifier comprises a maleic anhydride functionalized elastomeric ethylene copolymer, a maleic anhydride functionalized elastomeric ethylene/propylene copolymer, a terpolymer of ethylene, acrylic ester and maleic anhydride, a maleic anhydride grafted (MAH) polyolefin elastomer or combinations thereof.

In another embodiment, the thermoplastic composition further comprises additives such as lubricants, glass fillers, mineral fillers, plasticizers, pigments, dyes, antioxidants, heat stabilizers, hydrolysis stabilizers, nucleating agents, flame retardants, blowing agents and combinations thereof.

In another embodiment, the mineral fillers are selected from the group consisting of kaolin, clay, talc, and wollastonite, diatominte, titanium dioxide, mica, amorphous silica and combinations thereof.

In another embodiment, the glass fillers are selected from the group consisting of glass fiber, glass flakes, glass beads and combinations thereof.

In another embodiment, the glass fillers are hydrolysis resistant glass fibers coated with a sizing composition and organosilane coupling agents.

In another embodiment, the heat stabilizers are selected from the group consisting of hindered phenols, amine antioxidants, hindered amine light stabilizers (HALS), aryl amines, phosphorus based antioxidants, copper heat stabilizers, polyhydric alcohols, tripentaerythritol, dipentaerythritol, pentaerythritol and combinations thereof.

In another embodiment, the polyamide resin is selected from a group consisting of Nylon 6, Nylon 6,6, Nylon 6,12, Nylon 4,6, Nylon 6,10, Nylon 7, Nylon 10, Nylon 10, 10, Nylon 12, Nylon 12, 12, Nylon 6T, Nylon 6T/6I, Nylon 6T/DT, Nylon MXD-6 and combinations thereof.

In another embodiment, the polyamide resin is Nylon 6,6.

In another embodiment, the silicone from the silicone based additive blooms to the surface of the thermoplastic composition and provides a hydrophobic layer.

In another embodiment, the thermoplastic composition further comprises from about 0.1 to about 5.0 by weight of an olefin and maleic anhydride copolymer, wherein the an olefin and maleic anhydride copolymer has a molecular weight in the range of about 300 to about 1,000,000 and the ratio of olefin to maleic anhydride is 1:1. In another embodiment, the thermoplastic composition the olefin is ethylene. In another embodiment, the shear RV is greater than 1000 Pa when tested at a shear rate of 100 sec-1. In another embodiment, the shear RV is greater than 2000 Pa when tested at a shear rate of 30 sec-1.

In another embodiment, the polymer performance modifier is present in an amount from about 16% to about 18% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight.

In another embodiment, the polymer performance modifier is present in about 16% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, wherein the impact strength is at least 70 kJ/m2 when tested at room temperature.

In another embodiment, the polymer performance modifier is present in an amount from about 18% to about 22% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, wherein the impact strength is at least 80 kJ/m2 when tested at room temperature.

In another embodiment, the invention the polymer performance modifier is present at about 16% to about 22% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, wherein the tensile strength is at least 20 Mpa at 50% elongation when tested at 100% moisture saturation.

In another embodiment, the polymer performance modifier is present at about 16% to about 22% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, wherein no break was observed at 200% elongation when tested at 100% moisture saturation.

In another embodiment, the invention is a molded article comprising the thermoplastic composition disclosed above.

In another embodiment, the molded article is used in the field of the automotive industry.

In another embodiment, the molded article is used for blow molded or injection molded applications.

In another embodiment, the molded articles is used for pneumatic duct work, pipes, tubing, chemical containers, gas tanks, fasteners and snap fit parts, hinged parts, gears and bearings, sporting goods, ski bearings, sprinkler heads, driving barrels, microcellular foam processing, lawn mower parts or appliances.

In another embodiment of the current invention, there is a process taught for forming the thermoplastic composition of claim 1 comprising the steps of adding a polymer performance modifier and a silicone based additive to a polyamide resin and mixing the polymer modifier, silicone based additive and polyamide resin to form a high impact polymer.

In another embodiment, the of the current invention, there is a process taught for increasing the impact strength in a polymer comprising the steps of adding a polymer performance modifier and a silicone based additive comprising an ultrahigh molecular weight siloxane polymer to a polyamide resin and mixing the polymer modifier, silicone based additive and polyamide resin to form a high impact polymer, wherein the a high impact polymer has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and polymer modifier.

In another embodiment of the process, the polymer performance modifier comprises a maleic anhydride functionalized elastomeric ethylene copolymer, a maleic anhydride functionalized elastomeric ethylene/propylene copolymer, a terpolymer of ethylene, acrylic ester and maleic anhydride, a maleic anhydride grafted (MAH) polyolefin elastomer or combinations thereof.

In another embodiment of the process, the polyamide resin is Nylon 6,6.

In another embodiment of the current invention, a thermoplastic composition is disclosed comprising from about 50 to about 99 by weight percent of a polyamide resin; from about 1 to about 50 by weight percent of a polymer performance modifier; from 0.01 to about 25 by weight percent of a silicone based additive; and from about 0.1 to about 5.0 by weight of an olefin and maleic anhydride copolymer, wherein the an olefin and maleic anhydride copolymer has a molecular weight in the range of about 300 to about 1,000,000 and the ratio of olefin to maleic anhydride is 1:1. In another embodiment, the thermoplastic composition the olefin is ethylene. In another embodiment, the shear RV is greater than 1000 Pa when tested at a shear rate of 100 sec-1. In another embodiment, the shear RV is greater than 2000 Pa when tested at a shear rate of 30 sec-1.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a chart summarizing the impact strength of unreinforced nylon 6,6 resin with various amounts of a polymer performance modifier and a silicone based additive.

FIG. 2 is a chart summarizing the impact strength of unreinforced nylon 6,6 resin with various amounts of a polymer performance modifier and a silicone based additive tested at −40° C.

FIG. 3 is a chart summarizing the impact strength of unreinforced nylon 6,6 resin with various amounts of a polymer performance and a silicone based additive tested at room temperature.

FIG. 4 is a chart summarizing the tensile strength of unreinforced nylon 6,6 resin with various amounts of a polymer performance modifier and a silicone based additive tested after moisture conditioning.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a thermoplastic composition that comprises a polyamide resin, a polymer performance modifier and a silicone based additive. The resulting thermoplastic composition has an impact strength that is greater than the combination of the polyamide resin and polymer performance modifier alone and a tensile strength that is comparable the polyamide resin.

All patents, patent applications, test procedures, priority documents, articles, publications, manuals, and other documents cited herein are fully incorporated by reference to the extent such disclosure is not inconsistent with this invention and for all jurisdictions in which such incorporation is permitted.

In an exemplary embodiment of the current invention, the thermoplastic composition comprises from about 25 to about 99 by weight percent of a polyamide resin; from about 1 to about 50 by weight percent of a polymer performance modifier; and about from 0.01 to about 25 by weight percent of a silicone based additive. Due to the high impact strength and low flexibility of the thermoplastic composition, molded articles comprising the thermoplastic composition are useful for many industrial applications. One preferred use is in the automotive industry.

Other preferred uses of the current invention include, but are not limited to blow molded or injection molded applications, pneumatic duct work, pipes, tubing, chemical containers, gas tanks, fasteners and snap fit parts, hinged parts, gears and bearings, sporting goods, ski bearings, sprinkler heads, driving barrels, microcellular foam processing (i.e. Mucell® Technology), lawn mower parts or appliances.

In an exemplary embodiment of the current invention, the silicone based additive comprises an ultrahigh molecular weight siloxane polymer and may further comprise a binding agent. The ultrahigh molecular weight siloxane polymer is unfunctionalized and non-reactive with the polyamide resin. In addition, an unfunctionalized siloxane polymer cannot be considered as either a gel or an oil. Suitable binding agents for the silicone based additive include fumed silica. The silicone based additive may be provided in a pelletized silicone gum formulation. A commercially available formulation is sold under the name Genioplast® Pellet S by Wacker.

This invention is based on the unexpected and surprising finding that the impact performance of a thermoplastic composition containing a polyamide resin is greatly improved by the synergistic combination of a performance modifier and an ultrahigh molecular weight siloxane polymer. The thermoplastic composition of the present invention has been shown to undergo uniform deformation upon stress and loading. In addition, the thermoplastic composition of the present invention has improved impact resistance, toughness, low temperature ductility, fatigue resistance, wear resistance, resistance to necking, and elastic recovery. The thermoplastic composition of the present invention also provides high burst pressure and an improved surface appearance for glass filled resins.

This remarkable behavior of siloxane polymer is believed to be due to its immobility in the continuous phase of the nylon composition, which allows it evenly distribute throughout the thermoplastic composition. The high molecular weight nature prevents the siloxane polymer from migrating or diffusing to the surface, and eventually dissipating, that helps in dampening the impact energy in conjunction with the performance modifier. Gels or Oils, on the other hand, would tend to migrate to the surface because of very high diffusivity, especially at processing conditions. It has also been found that the silicone from the traditional silicone based additive blooms to the surface of the thermoplastic composition and provides a hydrophobic layer.

In another embodiment of the invention, the melt viscosity of the thermoplastic composition can be increased. In this embodiment, a thermoplastic composition is disclosed comprising from about 50 to about 99 by weight percent of a polyamide resin; from about 1 to about 50 by weight percent of a polymer performance modifier; from 0.01 to about 25 by weight percent of a silicone based additive; and from about 0.1 to about 5.0 by weight of an olefin and maleic anhydride copolymer, wherein the an olefin and maleic anhydride copolymer has a molecular weight in the range of about 300 to about 1,000,000 and the ratio of olefin to maleic anhydride is 1:1. Suitable olefins include any that are known in the art. In an exemplary embodiment of the current invention, the olefin is ethylene. A commercially available 1:1 copolymer of ethylene and maleic anhydride is sold under the name ZeMac® by Vertellus®. As described in Example 4, the shear viscosity can be increased to a range of about 1000 to about 2100 Pa when tested at a shear rate range from about 30 to about 100 sec⁻¹. At this melt viscosity, the thermoplastic composition can be used for blow molding and pipe extrusion applications.

Suitable polyamide resins that may be used for the current invention include any known polyamides in the art. These include aliphatic, semicrystalline, aromatic or semiaromatic nylon resins. The nylon resins are those prepared from starting materials of essentially a lactam or a diamine, and an aliphatic, semiaromatic or aromatic dicarboxylic acid. Suitable lactams include caprolactam and laurolactam. Suitable amines include tetramethylenediamine, hexamethylenediamine (HMD), 2-methylpentamethylenediamine, undecamethylenediamine, dodecamethylenediamine, 2,2,4-/2,4,4-trimethylhexamethylenediamine, 5-methylnonamethylenediamine, metaxylylenediamine (MXD), paraxylylenediamine and 2-Methyl-1,5-pentamethylenediamine (MPMD). Suitable dicarboxylic acids such include adipic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid (DDDA), terephthalic acid (TPA), isophthalic acid (IPA), 2-chloroterephthalic acid, 2-methylterephthalic acid, 5-methylisophthalic acid, 5-sodium-sulfoisophthalic acid, hexahydroterephthalic acid and hexahydroisophthalic acid. In the invention, nylon homopolymers or copolymers to be derived from those starting materials are used either singly or as their mixtures.

Specific examples of polyamide resins that are suitable for the current invention are polycapramide (nylon 6), polyundecanamide (nylon 11), polylauramide (nylon 12), polyhexamethylenadipamide (nylon 66), polytetramethylenadipamide (nylon 46), polyhexamethylenesebacamide (nylon 610), polyhexamethylenedodecamide (nylon 612), polyhexamethyleneterephthalamide/polycapramide copolymer (nylon 6T/6), polyhexamethyleneterephthalamide/polydodecanamide copolymer (nylon 6T/12), polyhexamethylenadipamide/polyhexamethyleneterephthalamide copolymer (nylon 66/6T), polyhexamethylenadipamide/polyhexamethylenisophthalamide copolymer (nylon 66/6I), polyhexamethylenadipamide/polyhexamethylenisophthalamide/-polycapramide copolymer (nylon 66/6I/6), polyhexamethylenadipamide/polyhexamethyleneterephthalamide/polyhexamethylenisophthalamide copolymer (nylon 66/6T/6I), polyhexamethyleneterephthalamide/-polyhexamethylenisophtha lamide copolymer (nylon 6T/6I), polyhexamethyleneterephthalamide/poly(2-methylpentamethylene)terephthalamide copolymer (nylon 6T/M5T), polyhexamethyleneterephthalamide/-polyhexamethylenesebacamide/polycapramide copolymer (nylon 6T/610/6), polyhexamethyleneterephthalamide/polydodecanamide/-polyhexamethylenadipamide copolymer (nylon 6T/12/66), polyhexamethyleneterephthalamide/polydodecanamide/-polyhexamethylenisophthalamide copolymer (nylon 6T/12/6I), poly m-xylylenadipamide (nylon MXD6), as well as their mixtures and copolymers, etc.

Especially preferred are nylon resins suitable for the current invention are Nylon 6, Nylon 6,6, Nylon 6,12, Nylon 4,6, Nylon 6,10, Nylon 7, Nylon 10, Nylon 10, 10, Nylon 12, Nylon 12, 12, Nylon 6T, Nylon 6I, Nylon DT, Nylon DI, Nylon MXD-6 and combinations or copolymers thereof. In another exemplary embodiment of the current invention the polyamide resin is Nylon 6,6.

The thermoplastic composition of the current invention has an impact strength value which is greater than the combination of the polyamide resin and the polymer performance modifier or the combination of the polyamide resin and the silicone based additive. In addition thermoplastic composition has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and the polymer performance modifier.

The thermoplastic composition of the current invention also comprises a polymer performance modifier. Suitable polymer performance modifiers include those known in the art that impart improved impact strength when combined with polyamide resins. U.S. Pat. Nos. 4,346,194, 6,579,581 and 7,671,127, herein incorporated by reference, teach nylon resins with impact modifying components. In an exemplary embodiment of the current invention the polymer modifier comprises an elastomeric polyolefinic polymer functionalized with an unsaturated carboxylic anhydride.

Suitable elastomers are polymers or copolymers of ethylene, propylene, octene with alkyl acrylate or alkyl methacrylate. Other suitable elastomers include styrene-butadiene two-block copolymers (SB), styrene-butadiene-styrene three-block copolymers (SBS), and hydrogenated styrene-ethene/butene-styrene three-block copolymers (SEBS). Other elastomers that may be used include terpolymers of ethylene, of propylene, and of a diene (EPDM rubber).

Suitable functional groups include carboxylic acid groups, carboxylic anhydride groups, carboxylic ester groups, carboxamide groups, carboximide groups, amino groups, hydroxy groups, epoxy groups, urethane groups, and oxazoline groups. Examples of suitable monomers for introducing the functional groups are maleic anhydride, itaconic acid, acrylic acid, glycidyl acrylate, and glycidyl methacrylate.

Suitable polymer performance modifiers are commercially available, such as that sold by Dow® under the name Amplify™ GR216 which is a maleic anhydride polyolefin elastomer. Another suitable commercially available polymer performance modifier is sold by Arkema® under the name Lotader® 4700 and is a random terpolymer of ethylene, ethyl acrylate and maleic anhydride. Another suitable commercially available polymer performance modifier is sold by ExxonMobil® under the name Exxelor™ VA 1840 and is a semi-crystalline ethylene copolymer functionalized with maleic anhydride. Yet another suitable commercially available performance modifier is sold by Arkema® under the name Oervac® IM300 and is a maleic anhydride modified low-density polyethylene. Other polymer performance modifiers are commonly used.

The thermoplastic composition of the current invention may further comprise additives such as lubricants, glass fillers, mineral fillers, plasticizers, pigments, dyes, antioxidants, heat stabilizers, hydrolysis stabilizers, nucleating agents, flame retardants, blowing agents and combinations thereof. Suitable mineral fillers can be selected from the group consisting of kaolin, clay, talc, and wollastonite, diatominte, titanium dioxide, mica, amorphous silica and combinations thereof. Suitable glass fillers are selected from the group consisting of glass fiber, glass flakes, glass beads and combinations thereof. The glass fibers may also be coated with a sizing composition and organosilane coupling agents to provide hydrolysis resistance. Suitable coated glass fibers are taught in U.S. Pat. Nos. 6,207,737, 6,846,855, 7,419,721 and 7,732,047, which are herein incorporated by reference. Suitable heat stabilizers are selected from the group consisting of hindered phenols, amine antioxidants, hindered amine light stabilizers (HALS), aryl amines, phosphorus based antioxidants, copper heat stabilizers, polyhydric alcohols, tripentaerythritol, dipentaerythritol, pentaerythritol and combinations thereof.

In one exemplary embodiment, the thermoplastic composition of the current invention is formed by adding a polymer performance modifier and a silicone based additive comprising an ultrahigh molecular weight siloxane polymer additive to a polyamide resin and mixing the polymer performance modifier, silicone based additive and polyamide resin to form a high impact polymer. The high impact polymer has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and polymer performance modifier. Suitable equipment for blending the polyamide resin, siloxane polymer and performance modifier include a twin-screw extruder, melt kneader or batch mixer. The thermoplastic composition is suitable for compounding or for use as a masterbatch.

As shown in Example 5, one aspect of the thermoplastic compositions of the current invention is increased lubricity. This increased lubricity results in reduced friction between moving parts which is ideal for uses such as gears, living hinges, syringe parts; medical devices, electronic connectors and the like.

In preferred embodiments the polymer performance modifier comprises a maleic anhydride functionalized elastomeric ethylene copolymer, a maleic anhydride functionalized elastomeric ethylene/propylene copolymer, a terpolymer of ethylene, acrylic ester and maleic anhydride, a maleic anhydride grafted (MAH) polyolefin elastomer or combinations thereof. In a preferred embodiment of this process, the polyamide resin is Nylon 6,6.

EXAMPLES

The following Examples demonstrate the present invention and its capability for use. The invention is capable of other and different embodiments, and its several details are capable of modifications in various apparent respects, without departing from the scope and spirit of the present invention. Accordingly, the Examples are to be regarded as illustrative in nature and non-limiting.

Comparative Example 1

TABLE 1 Control Nylon 66 (Average Values) Tensile Strength @ yield, Mpa 47-50 Strain @ yield, % 4.4 Strain @ break, % 34.2 Ten Mod, Mpa 1940-2000 R.T. Notched Charpy. kJ/m2 76

Table 1 shows the strength characteristic for INVISTA formulation nylon resin that contains 42-65% by weight nylon 6,6 composition having a copper iodide heat stabilizer and an aluminum stearate lubricant. The resin also contains 22% of a polymer performance modifier of ethylene copolymer functionalized with maleic anhydride (i.e.: Exxelor™ VA1840) and no silicon based additive.

Example 1

TABLE 2 1 2 3 4 5 6 7 3 9 10 11 12 A B C D E F G H J K L M Nylon 66 81.47 79.47 77.47 79.47 77.47 75.47 77.47 75.47 73.47 75.47 73.47 71.47 Exxelor VA1840 16 16 16 18 18 18 20 20 20 22 22 22 Shepherd 8:1:1 H

0.33 0.33 0.33 0.33 033 033 0.33 0.33 0.33 0.33 0.33 0.33 CNH-00509 1 1 1 1 1 1 1 1 1 1 1 1 UHMW Si

1 3 5 1 3 5 1 3 5 1 3 5 Al Stearate 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 Total 100 100 100 100 100 100 100 100 100 100 100 100 Notched Charpy, 48.4 72.3 79.2 68.1 83.2 98.8 80.7 90.7 96.4 90.3 98.6 103.1 kJ/m2 at R.T. Notched Charpy, 14.4 17.3 19.6 14.9 20.6 19.65 19.1 23.06 44.7 20.7 26.6 69.7 kJ/m2 at −40 C. TS @ yield, Mpa 56.7 53 50.4 53.3 50 47.7 50.5 47.7 45.5 48.3 45.2 43.4 Strain @ yield, % 5.4 5.5 5.9 6.4 6.2 5.8 6.6 6.7 9.4 6.8 10 29 Strain @ break, % 21.6 35.7 35.4 26.2 38.6 42.6 31 36.3 50.3 32.7 42 61 Ten Mod, Mpa 2117 2320 1990 2046 2005 1918 2255 1934 1941 1995 1827 2389

indicates data missing or illegible when filed

Table 2 summarizes the results from adding various amounts of a silicone based additive and polymer performance polymer additive to INVISTA formulation unreinforced nylon 6,6 resin. The silicone based additive added was pelletized silicone gum formulation sold under the name Genioplast® Pellet S by Wacker. The pellets contain about 65% by weight of ultra high molecular weight siloxane gum content. The polymer performance polymer additive was an ethylene copolymer functionalized with maleic anhydride sold by ExxonMobil® under the name Exxelor™ VA 1840. The results show that high level tough impact properties are achieved without sacrificing other properties such as flexural properties, tensile strength, modulus surface finish and tribology. For example, at room temperature (R.T.) and at 16% impact modifier and 5% siloxane gum loading an impact strength of 79.2 Kj/m2 and tensile strength of 50.5 Mpa was achieved. This is a significant increase from the impact strength from the comparative example at the same polymer performance modifier level (16.8 Kj/m2). In fact, the impact strength still remains higher than when the comparative example has an polymer performance modifier level of 22% (76.4 Kj/m2). FIG. 1 summarizes the comparison of the impact strength of the unreinforced INVISTA formulation nylon 6,6 resin at various loadings of Genioplast® Pellet S and Exxelor™ VA 1840 (tested at R.T.). As shown in FIG. 1, when the polymer performance modifier is present at about 16% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, the impact strength is at least about 70 kJ/m2 when tested at room temperature. In addition, when the polymer performance modifier is present in an amount from about 18% to about 22% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, the impact strength is at least about 80 kJ/m2 when tested at room temperature. In addition, the tensile strength of the sample remained substantially the same. It was shown that the tensile strength of the samples at various siloxane gum remained within 80% of that of the resin from the comparative example.

Example 2

FIG. 2 and FIG. 3 show samples of INVISTA formulation unreinforced nylon 6,6 resin that are combined with various amounts of silicone based additive and a polymer performance modifier. FIG. 2 shows the results at −40° C. and FIG. 3 shows the results at room temperature (R.T.). The silicone based additives were Genioplast® pellets. The polymer performance modifier was a maleic anhydride polyolefin elastomer sold by Dow® under the name Amplify™ GR 216. FIGS. 2 and 3 both show that a significant increase in impact strength greater can be achieved using the combination of the polymer performance modifier and siloxane gum additive. As shown in FIG. 2, when the polymer performance modifier is present in an amount from about 16% to about 22% by weight and the silicone based additive is present in an amount from about 1.0% to about 5.0% by weight, the impact strength is at least about 20 kJ/m2 when tested at −40° C.

Example 3

FIG. 4 shows samples of INVISTA formulation unreinforced nylon 6,6 resin that are combined with various amounts of silicone based additive and a polymer performance modifier. The silicone based additives were Genioplast® pellets. The polymer performance polymer additive was an ethylene copolymer functionalized with maleic anhydride sold by ExxonMobil® under the name Exxelor™ VA 1840. The specimens were conditioned in saturated moisture at 70° C. for 17 days in a closed container to achieve 100% saturation. The results are summarized in Table 3. As can be seen the tensile strength of the samples with 22% polymer performance modifier (21.9-23.7 Mpa) is well within 80% of the tensile strength of the sample with no silicone based additive (24.4 Mpa). FIG. 4 shows the tensile strength of the samples when tested at 50% elongation. In addition, no break was observed in the samples when tested at 200% elongation.

TABLE 3 Wt of specimen % MOI after Wt of absorbed conditioning in DAM @ 70 C. for TS @ Sample % Exxelor % IMD closed box at 70 specimen, 17 days yield, % Strain % Strain RB-041 VA 1840 additive deg C./17 day (gms) gms (100% RH) Mpa @ yield @ break A 16 1 10.3214 9.8046 5.28 27.2 50 no break @ 200% B 16 3 10.4348 9.832 6.14 25.7 50 no break @ 200% C 16 5 10.3537 9.7574 6.12 25.4 50 no break @ 200% D 18 1 10.2841 9.6958 6.07 25.3 50 no break @ 200% E 18 3 10.1927 9.6935 5.15 24.9 50 no break @ 200% F 18 5 10.2734 9.6823 6.11 23.6 50 no break @ 200% G 20 1 10.1459 9.6285 5.38 24.9 50 no break @ 200% H 20 3 10.1685 9.6507 5.37 24.1 50 no break @ 200% J 20 5 10.1585 9.6374 5.41 23.6 50 no break @ 200% K 22 1 10.188 9.6219 5.89 23.7 50 no break @ 200% L 22 3 10.0919 9.5358 5.84 22.7 50 no break @ 200% M 22 5 10.067 9.5174 5.78 21.9 50 no break @ 200% F11-0111 22 0 10.0517 9.4942 5.88 24.4 50 no break @ 200% ACS Lot

Example 4

Example 4 exhibits how the melt viscosity of the thermoplastic composition can be increased with the addition of a copolymer of ethylene and maleic anhydride. Table 4 compares the melt viscosity, which is tested by measuring the shear viscosity, of various resins. Sample 1 is an INVISTA formulation unreinforced nylon 6,6 resin that is combined with a silicone based additive and a polymer performance modifier. Sample 2 is an INVISTA formulation unreinforced nylon 6,6 resin that is combined with a silicone based additive, a polymer performance modifier and a 1:1 copolymer of ethylene and maleic anhydride. The silicone based additives were Genioplast® pellets. The polymer performance polymer additive was an ethylene copolymer functionalized with maleic anhydride sold by ExxonMobil® under the name Exxelor™ VA 1840. The 1:1 copolymer of ethylene and maleic anhydride is sold by Vertellus® under the name ZeMac®. Sample 3 is a comparative example showing the melt viscosity of a high density polyethylene (HDPE) resin. The shear viscosity was measured using a capillary rheometer at various shear rates. As shown in Table 4 below, the shear viscosity (and correspondingly the Melt Viscosity) of Sample 2 showed a significant increase over Sample 1 at lower shear rates.

TABLE 4 Sample 1 Sample 2 B G HDPE (180 C.) Nylon 6,6 70 69 Exxelor VA 1840 22 22 ZeMac 60 1 Wacker Pellet S 5 5 Cu based Heat 0.3 0.3 Stabilizer phenolic antioxidants 0.5 0.5 Carbon Black 2 2 Zn Stearate 0.2 0.2 Total 100 100 Shear Rate (sec −1) Shear Viscosity (Pa) 10040.2 30.5 43.5 35.1 5020.1 47.3 73.0 60.7 4016.0 53.1 85.7 69.7 3011.0 63.8 104.1 90.5 2006.6 79.7 136.8 121.9 1001.8 113.3 221.0 180.8 499.7 159.4 362.5 310.7 296.3 200.3 525.3 454.2 148.2 273.2 827.5 807.7 100.0 325.5 1052.3 1180.1 50.0 461.0 1480.5 1900.3 30.0 584.2 2062.8 2597.4

Example 5

Example 5 exhibits how the insertion-extraction (also known as “push-pull”) performance of the thermoplastic composition can be improved with the addition of a polymer performance modifier and silicone based additive. Table 5 compares the push-pull performance of the connector parts made with modified thermoplastic resinlabeled “T3000HSL” with a connector parts molded from a similar competitive grade labeled “H6004”. The T3000HSL is a commercially available TORZEN® PA66 resin brand manufactured by INVISTA Engineering Polymer Solutions. The T3000HSL product datasheet can be referenced at the INVISTA internet site: http://eps.invista.com/documents/tds/TORZEN.

The insertion-extraction performance was measured at 5.0 inches/min test speed. The unit of measure was lbs in all tests. The test was performed by inserting and extracting the pin of the connector through a 8.1 mm hole. Table 5 below summarizes the test results for the samples tested.

TABLE 5 Competitive resin INVISTA resin “H6004” “T3000HSL” Push Push (Insertion) Pull (Extraction) (Insertion) Pull (Extraction) force force force force (lbs) (lbs) (lbs) (lbs) Average 17.93 148.82 16.29 143.8 Range 4.3 15.3 2.3 6.9 Max 20.0 158.3 17.4 146.7 Min 15.7 143.0 15.1 139.8

The measured performance data given in Table 5 undoubtedly shows an overall push-pull performance improvement, i.e., easy push and easy pull indicated by the lower values for T3000HSL as compared against the comparative H6004 specimen.

It should be noted that ratios, concentrations, amounts, and other numerical data may be expressed herein in a range format. It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a concentration range of “about 0.1% to about 5%” should be interpreted to include not only the explicitly recited concentration of about 0.1 wt % to about 5 wt %, but also the individual concentrations (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within the indicated range. The term “about” can include ±1%, ±2%, ±3%, ±4%, ±5%, ±8%, or ±10%, of the numerical value(s) being modified. In addition, the phrase “about ‘x’ to ‘y’” includes “about ‘x’ to about ‘y’”.

While the illustrative embodiments of the invention have been described with particularity, it will be understood that the invention is capable of other and different embodiments and that various other modifications will be apparent to and may be readily made by those skilled in the art without departing from the spirit and scope of the invention. Accordingly, it is not intended that the scope of the claims hereof be limited to the examples and descriptions set forth herein but rather that the claims be construed as encompassing all the features of patentable novelty which reside in the present disclosure, including all features which would be treated as equivalents thereof by those skilled in the art to which the invention pertains. 

What is claimed:
 1. A process for increasing the impact strength in a polymer comprising the steps of adding a polymer performance modifier and a silicone based additive comprising an ultrahigh molecular weight siloxane polymer to a polyamide resin and mixing the polymer performance modifier, silicone based additive and polyamide resin to form a high impact polymer, wherein the a high impact polymer has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and polymer performance modifier.
 2. The process of claim 1 wherein the polymer performance modifier comprises a maleic anhydride functionalized elastomeric ethylene copolymer, a maleic anhydride functionalized elastomeric ethylene/propylene copolymer, a terpolymer of ethylene, acrylic ester and maleic anhydride, a maleic anhydride grafted (MAH) polyolefin elastomer or combinations thereof.
 3. The process of claim 1 wherein the polyamide resin is Nylon 6,6.
 4. A thermoplastic composition comprising from about 50 to about 99 by weight percent of a polyamide resin; from about 1 to about 50 by weight percent of a polymer performance modifier; from 0.01 to about 25 by weight percent of a silicone based additive; and from about 0.1 to about 5.0 by weight of an olefin and maleic anhydride copolymer, wherein the an olefin and maleic anhydride copolymer has a molecular weight in the range of about 300 to about 1,000,000 and the ratio of olefin to maleic anhydride is 1:1.
 5. The thermoplastic composition of claim 4 wherein the thermoplastic composition has an impact strength value which is greater than the combination of the polyamide resin and the polymer performance modifier or the combination of the polyamide resin and the silicone based additive.
 6. The thermoplastic composition of claim 4 wherein the thermoplastic composition has an ultimate tensile strength that is at least 80% that of the combination of the polyamide resin and the polymer performance modifier.
 7. The thermoplastic composition of claim 4 wherein the silicone based additive comprises an ultrahigh molecular weight siloxane polymer.
 8. The thermoplastic composition of claim 7 wherein the ultrahigh molecular weight siloxane polymer is unfunctionalized and non-reactive with the polyamide resin.
 9. The thermoplastic composition of claim 4 wherein the polymer performance modifier comprises an elastomeric polyolefinic polymer functionalized with an unsaturated carboxylic anhydride.
 10. The thermoplastic composition of claim 4 wherein the polymer performance modifier comprises a maleic anhydride functionalized elastomeric ethylene copolymer, a maleic anhydride functionalized elastomeric ethylene/propylene copolymer, a terpolymer of ethylene, acrylic ester and maleic anhydride, a maleic anhydride grafted (MAH) polyolefin elastomer or combinations thereof.
 11. The thermoplastic composition of claim 4 wherein the olefin is ethylene.
 12. The thermoplastic composition of claim 4 wherein the shear RV is greater than 1000 Pa when tested at a shear rate of 100 sec-1.
 13. The thermoplastic composition of claim 4 wherein the shear RV is greater than 2000 Pa when tested at a shear rate of 30 sec-1.
 14. The thermoplastic composition of claim 4 further comprising additives such as lubricants, glass fillers, mineral fillers, plasticizers, pigments, dyes, antioxidants, heat stabilizers, hydrolysis stabilizers, nucleating agents, flame retardants, blowing agents and combinations thereof.
 15. The thermoplastic composition of claim 4 wherein the polyamide resin is selected from a group consisting of Nylon 6, Nylon 6,6, Nylon 6,12, Nylon 4,6, Nylon 6,10, Nylon 7, Nylon 10, Nylon 10, 10, Nylon 12, Nylon 12, 12, Nylon 6T, Nylon 6T/6I, Nylon 6T/DT, Nylon MXD-6 and combinations thereof.
 16. The thermoplastic composition of claim 4 wherein the polyamide resin is Nylon 6,6.
 17. The thermoplastic composition of claim 4 wherein the silicone from the silicone based additive blooms to the surface of the thermoplastic composition and provides a hydrophobic layer.
 18. A molded article comprising the thermoplastic composition claim
 4. 19. The molded article of claim 18 wherein the molded article is used in the field of the automotive industry.
 20. The molded article of claim 18 wherein the molded article is formed by blow molded or injection molded applications.
 21. The molded article of claim 18 wherein the molded articles is used for pneumatic duct work, pipes, tubing, chemical containers, gas tanks, fasteners and snap fit parts, hinged parts, gears and bearings, sporting goods, ski bearings, sprinkler heads, driving barrels, microcellular foam processing, lawn mower parts or appliances. 